146 related articles for article (PubMed ID: 20359100)
1. [Analysis of deafness gene mutations by gene chip and its clinical significance].
Zhang H; Liu Y; Wang Y; Li G; Luo Z; Jiang Pf; Li F; Wang S; Deng K
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2009 Nov; 23(22):1032-5. PubMed ID: 20359100
[TBL] [Abstract][Full Text] [Related]
2. [Screening of common deafness gene mutations in 17 000 Chinese newborns from Chengdu based on microarray analysis].
Lyu K; Xiong Y; Yu H; Zou L; Ran L; Liu D; Yin Q; Xu Y; Fang X; Song Z; Huang L; Tan D; Zhang Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):547-52. PubMed ID: 25297577
[TBL] [Abstract][Full Text] [Related]
3. Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China.
Jiang Y; Huang S; Deng T; Wu L; Chen J; Kang D; Xu X; Li R; Han D; Dai P
PLoS One; 2015; 10(8):e0135088. PubMed ID: 26252218
[TBL] [Abstract][Full Text] [Related]
4. [DNA microarray screening analysis in children with profound hearing impairment in Hubei province].
Zhan Y; Wu X; Hu Y; Huang X; Duan J; Chen H; Jin J; Li D; Xie W; Kong W
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2014 May; 28(10):680-4. PubMed ID: 25129964
[TBL] [Abstract][Full Text] [Related]
5. Mutation analysis of common GJB2, SCL26A4 and 12S rRNA genes among 380 deafness patients in northern China.
Pan J; Xu P; Tang W; Cui Z; Feng M; Wang C
Int J Pediatr Otorhinolaryngol; 2017 Jul; 98():39-42. PubMed ID: 28583500
[TBL] [Abstract][Full Text] [Related]
6. Developing regional genetic counseling for southern Chinese with nonsyndromic hearing impairment: a unique mutational spectrum.
Chen K; Zong L; Liu M; Wang X; Zhou W; Zhan Y; Cao H; Dong C; Tang H; Jiang H
J Transl Med; 2014 Mar; 12():64. PubMed ID: 24612839
[TBL] [Abstract][Full Text] [Related]
7. [Analysis common gene mutation spots of 127 non-syndromic deafness natients in Guangxi Drovince].
Liu S; Xu L; Chen B; Liu M; Qu S; Liang J; Tang F; Shi M; Peng L; Jing Y; Li F; Liang Y
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov; 29(22):1954-8. PubMed ID: 26911057
[TBL] [Abstract][Full Text] [Related]
8. [Evaluation of deaf-mute patients with sensitive deafness gene screening in Shandong province].
Ji YB; Han DY; Wang DY; Zhou Y; Zhao C; Wang H; Lan L; Wang QJ
Zhonghua Yi Xue Za Zhi; 2009 Sep; 89(36):2531-5. PubMed ID: 20137612
[TBL] [Abstract][Full Text] [Related]
9. Common molecular etiology of patients with nonsyndromic hearing loss in Tibetan, Tu nationality, and Mongolian patients in the northwest of China.
Yang XL; Bai-Cheng X; Chen XJ; Pan-Pan B; Jian-Li M; Xiao-Wen L; Zhang ZW; Wan D; Zhu YM; Guo YF
Acta Otolaryngol; 2013 Sep; 133(9):930-4. PubMed ID: 23834103
[TBL] [Abstract][Full Text] [Related]
10. Genetic mutations in non-syndromic deafness patients in Hainan Province have a different mutational spectrum compared to patients from Mainland China.
Huang B; Han M; Wang G; Huang S; Zeng J; Yuan Y; Dai P
Int J Pediatr Otorhinolaryngol; 2018 May; 108():49-54. PubMed ID: 29605365
[TBL] [Abstract][Full Text] [Related]
11. [Common gene mutations study in Uyghur population with deafness in Kashgar region of Xinjiang].
Chen Y; Tudi M; Lu HL; Jiang D; Zhao J; Hu B; Kuyaxi P; Zhang H
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 Mar; 46(3):205-8. PubMed ID: 21575411
[TBL] [Abstract][Full Text] [Related]
12. Mutation analysis of common deafness genes among 1,201 patients with non-syndromic hearing loss in Shanxi Province.
Zhou Y; Li C; Li M; Zhao Z; Tian S; Xia H; Liu P; Han Y; Ren R; Chen J; Jia C; Guo W
Mol Genet Genomic Med; 2019 Mar; 7(3):e537. PubMed ID: 30693673
[TBL] [Abstract][Full Text] [Related]
13. [Genetic analysis and prenatal diagnosis for non-syndromic hearing impairment].
Wang L; Zhao HR; Liao S; Yang YL; Li T; Zhang B; Ding XB; Ma S; Liu HJ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Oct; 30(5):518-21. PubMed ID: 24078562
[TBL] [Abstract][Full Text] [Related]
14. Newborn Screening of Genetic Mutations in Common Deafness Genes With Bloodspot-Based Gene Chip Array.
He X; Li X; Guo Y; Zhao Y; Dong H; Dong J; Zhong L; Shi Z; Zhang Y; Soliman M; Song C; Zhao Z
Am J Audiol; 2018 Mar; 27(1):57-66. PubMed ID: 29234782
[TBL] [Abstract][Full Text] [Related]
15. [An analysis of the mutation in GJB2,GJB3,SLC26A4 and mtDNA12SrRNA in new born].
Chai F; Zhao HL; Qiu SQ
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2017 May; 31(9):664-666. PubMed ID: 29871341
[No Abstract] [Full Text] [Related]
16. [Diagnostic methods and clinic application for mtDNA A1555G and GJB2 and SLC26A4 genes in deaf patients].
Dai P; Yu F; Kang DY; Zhang X; Liu X; Mi WZ; Cao JY; Yuan HJ; Yang WY; Wu BL; Han DY
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2005 Oct; 40(10):769-73. PubMed ID: 16408730
[TBL] [Abstract][Full Text] [Related]
17. Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China.
Duan SH; Zhu YM; Wang YL; Guo YF
Acta Otolaryngol; 2015 Jun; 135(6):586-91. PubMed ID: 25761933
[TBL] [Abstract][Full Text] [Related]
18. [Molecular etiology analysis among students with profound hearing loss in a special education school in Yangzhou].
Peng X; Li X; Xu L; Guan B; Zhang J; Yu A
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 Jul; 26(13):577-80. PubMed ID: 23002639
[TBL] [Abstract][Full Text] [Related]
19. [Analysis of common mutations of deafness-related genes in 2725 newborns].
Yu H; Liu D; Yang J; Wu Z; Sun D; Ma W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):335-8. PubMed ID: 26037344
[TBL] [Abstract][Full Text] [Related]
20. GJB2, SLC26A4, and mitochondrial DNA12S rRNA hot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China.
Ma Y; Xiao Y; Bai X; Zhang F; Zhang D; Xu X; Xu L; Wang H
Acta Otolaryngol; 2016 Aug; 136(8):800-5. PubMed ID: 27066914
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]